Identity
- Trade Name
- Medex FDA UDI
- Generic Name
- Electric infusion pump administration set, single-use FDA UDI
- Model / Reference
- MX20887 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10351688508591 FDA UDI
- FDA Product Code
- FPA FDA UDIFPB FDA UDIFMG FDA UDI
- GMDN Term
- Electric infusion pump administration set, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Electric infusion pump administration set, single-use
Medex by Icu Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Electric infusion pump administration set, single-use.
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Cleared under the same submission
K782168 also covers:
K790314 also covers:
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
K943897 also covers:
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
- Medex — ICU MEDICAL, INC.
K944208 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Icu Medical, Inc.
Sources (1)
- FDA UDI e5645eca-0581-43b5-8bc5-31bc655a016f 33 fields · synced May 30, 2026